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Completed

NCT Number: NCT04039906

A Single-institutional Study to Assess the Time Efficiency and Working Satisfaction Using ANDY(Automatic Needle Destroyer)

Evaluate the efficiency of adopting the automated needle processing system by evaluating efficiency, usability and safety when using ANDY(Automatic Needle Destroyer). Install ANDY(Automatic Needle Destroyer) in the ER, and evaluate the system by comparing the efficiency of the work, usability, actual decrease ratio of needlestick injury between using the automated needle processing system and not using it.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Samsung Medical Center

Seoul, South Korea

About this study

  • Background The most frequent occupational injury is exposure to blood and fluid by needlestick injury. Needlestick injuries can result in serious infections if appropriate infection control measures are not taken promptly.

Since the use of safety devices are not popularly used, the needle and syringe are mostly taken into pieces by physical ways. There are some cases that the needle and syringe is not separated, and the entire syringe can be put directly into the waste container. There is also a problem that it takes a lot of time and efforts to remove needles from syringes. In addition, the existing safety mechanism is physical methods such as pulling out the needle, damaging or cutting the needle, or using heat to the needle, or melting it by using chemicals. It is a semi-manual since you have to wait holding the syringe during the process, and it is inconvenient to use considering a busy medical environment.

Therefore, we developed ANDY(Automatic Needle Destroyer) that can be introduced at a convenient and reasonable cost, and try to objectively evaluate the utility of ANDY in a clinical environment.

  • Purpose The purpose of this study is to Evaluate the efficiency of adopting the automated needle processing system by evaluating efficiency, usability and safety of the system.
  • Design : RCT (randomized controlled trial)
  • Setting: EMERGENCY CENTER at the Samsung Medical Center
  • Enrollment : 129 medical staffs in the ER. 10ea ANDY and 10ea of Existing waste containers(needle box)
  • Intervention :

6-1) 1st Week : Removal of needle with existing method

  • Record the time required for the needle removal procedure by photographing the needle removal procedure during 24 hours/7 days.
  • Identify the number of syringes processed by existing method.
  • Do survey after 1st week

6-2) 2nd week: Prepare for using ANDYs

  • Provide clinicians with instruction how to use ANDY
  • Install 10 ANDYs in the ER.

6-3) 3rd week : Removal of needle with using ANDYs

  • Record the time required for the needle removal procedure by photographing the needle removal procedure during 24 hours/7 days.
  • Identify the number of syringes processed by ANDY.
  • After 3rd week, do survey and interview 15 people selected by the convenient sample method. By interviewing, collect information of overall experience after using automated needle processing system, how long their hospital working experience is, and other information or systems the interviewees feel those are necessary.
  • Scoring: By the answers of the Questionnaire of Satisfaction (SUS and adjective score)
  • Study period : 3 weeks
  • Satisfaction survey: SUS and adjective score

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • medical staff of the ER
  • adult ER medical staff over 19 years of age
  • A subject who voluntarily agrees and signs

Exclusion criteria

•A subject who did not agree with this study

Treatment and study plan

Removal of needle with using ANDYs

Device
  • ANDY will be provided to medical staffs to be use in removal needles from syringes during 7 days
  • Record the time required for the needle removal procedure by photographing the needle removal procedure during 24 hours/7 days.

Identify the number of syringes processed by ANDY.

  • After 3rd week, do survey and interview 15 people selected by the convenient sample method. By interviewing, collect information of overall experience after using automated needle processing system, how long their hospital working experience is, and other information or systems the interviewees felt those are necessary.

Primary outcomes

  1. Time Efficiency: Comparing the time required to remove the needle from syringe for assessing change in time between using automated needle processing system or not

    Time frame: [1st Week] : Removal of needle in accordance with existing method, [3rd week] : using a ANDY(automated needle processing system)

    • Comparison of the required time(second) to remove the needle between using the automated needle processing system and not using it.

Secondary outcomes

  1. Usability: Comparing the SUS score for assessing the change in usability between using automated needle processing system or not

    Time frame: [1st Week] : Removal of needle in accordance with existing method, [3rd week] : using a ANDY(automated needle processing system)

    • Comparison of the usability between using the automated needle processing system and not using it by doing survey after 1st week and 3rd week and Interview after 3rd week( Scoring by the answers of the Questionnaire of Satisfaction (SUS) and adjective score)
  2. Safety: Comparing the number of accidents of the needlestick injuries between using automated needle processing system or not

    Time frame: [1st Week] : Removal of needle in accordance with existing method, [3rd week] : using a ANDY(automated needle processing system)

    • Comparison of the number of accidents of the needlestick injuries between using the automated needle processing system and not using it.

Sponsors and collaborators

Lead sponsor

Samsung Medical Center

Other

Registry information

Official study title

A Single-institutional Study to Assess the Impact of ANDY(Automatic Needle Destroyer) to the Medical Staffs in Terms of Working Efficiency Assessed by Working Time and Satisfaction Assessed by Usability and Safety Using SUS Score and Survey

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Jul 31, 2019
Registry last updated
Dec 3, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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